Package 11822-6440-1

Brand: pain reliever extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 11822-6440-1
Digits Only 1182264401
Product NDC 11822-6440
Description

237 mL in 1 BOTTLE, PLASTIC (11822-6440-1)

Marketing

Marketing Status
Discontinued 2026-05-29
Brand pain reliever extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23fc9191-f012-4087-95d0-af77f35e5434", "openfda": {"upc": ["0011822644013"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["b628a3d1-4534-453c-ac5a-573325662ddc"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (11822-6440-1)", "package_ndc": "11822-6440-1", "marketing_end_date": "20260529", "marketing_start_date": "20200131"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "11822-6440_23fc9191-f012-4087-95d0-af77f35e5434", "dosage_form": "LIQUID", "product_ndc": "11822-6440", "generic_name": "Acetaminophen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260529", "marketing_start_date": "20200131"}